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Journal Abstract Search


942 related items for PubMed ID: 27212418

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  • 24. A novel NF1 mutation in a Chinese patient with giant café-au-lait macule in neurofibromatosis type 1 associated with a malignant peripheral nerve sheath tumor and bone abnormality.
    Tong HX, Li M, Zhang Y, Zhu J, Lu WQ.
    Genet Mol Res; 2012 Aug 29; 11(3):2972-8. PubMed ID: 22869071
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  • 29. Ectropion Uveae in neurofibromatosis type 1: a new manifestation.
    Iacovino C, Miraglia E, Moramarco A, Corbo G, Lambiase A, Giustini S.
    Clin Ter; 2021 May 05; 172(3):206-208. PubMed ID: 33956037
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  • 30. Family with Legius syndrome (neurofibromatosis type 1-like syndrome).
    Sakai N, Maeda T, Kawakami H, Uchiyama M, Harada K, Tsuboi R, Mitsuhashi Y.
    J Dermatol; 2015 Jul 05; 42(7):703-5. PubMed ID: 25981987
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  • 31. Phenotypic variability among café-au-lait macules in neurofibromatosis type 1.
    Boyd KP, Gao L, Feng R, Beasley M, Messiaen L, Korf BR, Theos A.
    J Am Acad Dermatol; 2010 Sep 05; 63(3):440-7. PubMed ID: 20605257
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  • 33. Value of a café-au-lait macules screening clinic: Experience from The Hospital for Sick Children in Toronto.
    Albaghdadi M, Berseneva M, Pennal A, Wan S, Matviychuk D, Shugar A, Kannu P, Lara-Corrales I.
    Pediatr Dermatol; 2022 Mar 05; 39(2):205-210. PubMed ID: 35178768
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  • 38. [Anxiety disorders in type 1 neurofibromatosis: A case report].
    Fekih-Romdhane F, Othman S, Sahnoun C, Helayem S, Abbes Z, Bouden A.
    Arch Pediatr; 2015 Sep 05; 22(9):956-60. PubMed ID: 26228808
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